Cleared Traditional

K012923 - ARTHREX FIBERWIRE, USP SIZE 5, MODEL AR-7201

K012923 is an FDA 510(k) clearance for ARTHREX FIBERWIRE, manufactured by Arthrex, Inc.. The device is a Class 2 General & Plastic Surgery device with product code GAT cleared through the Traditional 510(k) pathway after a 34-day FDA review.

K012923 · Arthrex, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 2001
Decision
34d
Days
Class 2
Risk

K012923 is an FDA 510(k) clearance for the ARTHREX FIBERWIRE, USP SIZE 5, MODEL AR-7201. Classified as Suture, Nonabsorbable, Synthetic, Polyethylene (product code GAT), Class II - Special Controls.

Submitted by Arthrex, Inc. (Naples, US). The FDA issued a Cleared decision on October 4, 2001 after a review of 34 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.5000 - the FDA general and plastic surgery device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Arthrex, Inc. devices

FDA 510(k) Submission Details - K012923

510(k) Number K012923 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 31, 2001
Decision Date October 04, 2001
Days to Decision 34 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
81d faster than avg
Panel avg: 115d · This submission: 34d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GAT Device Classification - Class 2, Special Controls

Product Code GAT Suture, Nonabsorbable, Synthetic, Polyethylene
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.5000
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - GAT Suture, Nonabsorbable, Synthetic, Polyethylene

All 147
Devices cleared under the same product code (GAT) and FDA review panel - the closest regulatory comparables to K012923.
ARTHREX FIBERWIRE IN USP SIZES
K021434 · Arthrex, Inc. · Nov 2002
COTTONY II, SILKY II POLYDEK & TEVDEK II POLYESTER SUTURE
K021019 · Genzyme Corp. · Jun 2002
LIFESTITCH SUTURING DEVICE
K013990 · Edwards Lifesciences, LLC · Feb 2002
PREMICRON NONABSORBABLE PET SURGICAL SUTURE
K012201 · Aesculap, Inc. · Sep 2001
ARTHREX FIBERWIRE, MODEL SPU-02NB-3800
K010673 · Arthrex, Inc. · May 2001
POLYESTER NONABSORBABLE SURGICAL SUTURES URP
K001172 · Cp Medical · Jun 2000